International safety notice
Safety Notice/Recall for the Bard Lifestent Vascular Stent System, Angiomed
Germany / BfArM · DEU · Jan 19, 2011
Key facts
| Title | Safety Notice/Recall for the Bard Lifestent Vascular Stent System, Angiomed |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Bard Lifestent Vascular Stent System, Angiomed |
| Manufacturer | Safety Notice/Recall for the Bard Lifestent Vascular Stent System, Angiomed |
| Models | EX062003L, ETUEN08一一, …3U0=D, 2010-018, EX062001L, EX072001L, EX072003L, ØLLLEN02 |
| Date | Jan 19, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1